Tal Adit, Gunawardana-Zeigler Shimara, Peng Da, Tan Yuqi, Perez Natalia Munoz, Offenbacher Rachel, Kastner Laurel, Ciero Paul, Randolph Matthew E, Gong Yun, Deng Hong-Wen, Cahan Patrick, Loeb David M
bioRxiv. 2024 Dec 11:2024.12.10.627181. doi: 10.1101/2024.12.10.627181.
Osteosarcoma (OS) is the most common primary malignant bone tumor in childhood. Patients who present with metastatic disease at diagnosis or relapse have a very poor prognosis, and this has not changed over the past four decades. The Wnt signaling pathway plays a role in regulating osteogenesis and is implicated in OS pathogenesis. DKK-1 inhibits the canonical Wnt signaling pathway, causing inhibition of osteoblast differentiation and disordered bone repair. Our lab previously demonstrated that a monoclonal antibody against DKK-1 prevented metastatic disease in a mouse model. This study expands upon those findings by demonstrating similar results with a small molecule inhibitor of DKK-1, WAY262611, both and . WAY262611 was evaluated on osteosarcoma cell lines, including proliferation, caspase activation, cell cycle analysis, and signaling pathway activation. We utilized our orthotopic implantation-amputation model of osteosarcoma metastasis to determine the impact of WAY262611 on primary tumor progression and metastatic outgrowth of disseminated tumor cells. Differentiation status was determined using single cell RNA sequencing. We show here that WAY262611 activates canonical Wnt signaling, enhances nuclear localization and transcriptional activity of beta-catenin, and slows proliferation of OS cell lines. We also show that WAY262611 induces osteoblastic differentiation of an OS patient-derived xenograft , as well as inhibiting metastasis. This work credentials DKK-1 as a therapeutic target in OS, allowing for manipulation of the Wnt signaling pathway and providing preclinical justification for the development of new biologics for prevention of osteosarcoma metastasis.
骨肉瘤(OS)是儿童期最常见的原发性恶性骨肿瘤。诊断时或复发时出现转移性疾病的患者预后极差,且在过去四十年中这一情况并未改变。Wnt信号通路在调节骨生成中起作用,并与骨肉瘤发病机制有关。DKK-1抑制经典Wnt信号通路,导致成骨细胞分化受抑制和骨修复紊乱。我们实验室先前证明,一种针对DKK-1的单克隆抗体可预防小鼠模型中的转移性疾病。本研究通过用DKK-1的小分子抑制剂WAY262611证明类似结果,扩展了这些发现,包括在 和 方面。对WAY262611进行了骨肉瘤细胞系评估,包括增殖、半胱天冬酶激活、细胞周期分析和信号通路激活。我们利用骨肉瘤转移的原位植入-截肢模型来确定WAY262611对原发性肿瘤进展和播散肿瘤细胞转移生长的影响。使用单细胞RNA测序确定分化状态。我们在此表明,WAY262611激活经典Wnt信号,增强β-连环蛋白的核定位和转录活性,并减缓骨肉瘤细胞系的增殖。我们还表明,WAY262611诱导骨肉瘤患者来源异种移植瘤的成骨细胞分化,以及抑制转移。这项工作证明DKK-1是骨肉瘤的治疗靶点,允许对Wnt信号通路进行调控,并为开发预防骨肉瘤转移的新生物制剂提供临床前依据。